Office Secretary - Center for Clinical Research-临床研究中心办公室秘书-北京-01122
岗位职责 • Coordinate on SFDA & CFDA drug site application process • Development and maintain CCR office management system • Coordinate IRB communication, application process • Coordinate clinical research related training • Refine and maintain CCR related website • Coordinate with personnel related to CCR office • Coordinate relevant meetings with different departments • Attend GCP trainings as required • Other duties as assigned 任职条件 • Holder of Bachelor's Degree or Mater's Degree in Bio-chem, Chemistry,Pharmacy, Laboratory, Medical, Nurse or other relevant majors • Previous research or clinical experience; familiar with policies andprograms related to the clinical research • Familiar with medical terminology and comfortable in working inmedical setting on day-to-day basis • Ability to comply with regulated protocol, policies and procedures;able to organize and prioritize tasks • Effective oral and written communication skills in English and Chinese • Skill in exercising initiative, judgment, problem solving. • Professional telephone etiquette • Self-motivated, strong organizational skills, and the initiative towork independently to meet deadlines 职位概述 Summary of Responsibilities: Will play an important role in assisting with the continued growth ofCenter for Clinical Research and Institutional Review Board, includingthe CFDA drug site application process and daily communication andmanagement of the office 部门概述 CENTER FOR CLINICAL RESEARCH
Mission Statements The Center for Clinical Research (CCR) of the United Family Healthcare(UFH) promotes and oversees clinical research conducted at all the UFHfacilities. Clinical research means any systematic investigation thatinvolves human subjects.
The UFH Center for Clinical Research promotes and assists investigators,at all the UFH sites in China, to design, conduct and report of clinicalresearch projects. These projects may include, but not limited to, casereports, retrospective analysis, clinical trials of drugs and devices,and epidemiological studies. These projects may be UFHinvestigator-initiated studies, collaborated studies with otherinstitutions, or studies sponsored by private companies or governmental agencies.